OBO ID: DOID:0060427
Term Name: chromosome Xp21 deletion syndrome Search Ontology:
Synonyms:
  • complex glycerol kinase deficiency
  • monosomy Xp21
  • Xp21 microdeletion syndrome
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region. https://pubmed.ncbi.nlm.nih.gov/17089405/
References:
Ontology: Human Disease   ( DOID:0060427 )
Relationships
is a type of:
OTHER chromosome Xp21 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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